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A single-cylinder, spark-ignited engine was run on a certification test gasoline to saturate the oil in the sump with fuel through exposure to blow-by gas. The sump volume was large relative to production engines making its absorption-desorption time constant long relative to the experimental time. The engine was motored at 1500 RPM, 90° C coolant and oil temperature, and 0.43 bar MAP without fuel flow. Exhaust HC concentrations were measured by on-line FID and GC analysis. The total motoring HC emissions were 150 ppmC1; the HC species distribution was heavily weighted to the low-volatility components in the gasoline. No high volatility components were visible. The engine was then fired on isooctane fuel at the above conditions, producing a total engine-out HC emission of 2300 ppmC1 for Φ = 1.0 and MBT spark timing.

Atmospheric modelers and development engineers need accurate measures of NO2 emissions from motor vehicles. Due to the oxidative reaction of oxygen with NO, these measurements (typically taken from a bag sample) can be inaccurate if care is not taken to minimize the sample residence time in the bags. This reaction occurs slowly at low NO concentrations, however, at higher NO concentrations the reaction can rapidly speed up (for example, 50 ppm NO will experience a 10% concentration reduction in 6.5 minutes). This report explores the factors contributing to this artifact for emissions test cells. Estimates of the error in NO2 emission rate measurements for several scenarios are presented. Additionally, kinetic expressions of the reaction rate are shown to be fairly accurate for our test conditions, but should not be used in general without verification of the non-existence of competing, hindering or accelerating species within the sample bag.

The use of Selective Catalytic Reduction (SCR) for NOx emissions control has resulted in a new challenge for the emissions measurement community. Most SCR systems require injection of urea or ammonia into the exhaust stream. Residual ammonia present in vehicle exhaust can have deleterious effects on NOx analyzers using chemiluminescent detectors (CLD). Ammonia can poison converter catalysts in CLD NOx analyzers and may react with NO2 across the converter. Both of these issues lead to erroneous NOx measurements, as well as increased maintenance costs and downtime. This paper will describe the development and use of a low-cost, simple ammonia scrubber that can easily be integrated into sampling systems and requires little change in test cell maintenance procedures. Validation results show the scrubber to have capacity sufficient to last for a full day of testing of typical vehicles.

FTP emissions tests on a passenger vehicle equipped with a 1.8 L IDI turbo-charged diesel engine show that the mass emissions of particles decrease by (36±8)% when 16.6% dimethoxymethane (DMM) by volume is added to a diesel fuel. Particle size measurements reveal log-normal accumulation mode distributions with number weighted geometric mean diameters in the 80 - 100 nm range. The number density is comparable for both base fuel and the DMM/diesel blend; however, the distributions shift to smaller particle diameter for the blend. This shift to smaller size is consistent with the observed reduction in particulate mass. No change is observed in NOx emissions. Formaldehyde emissions increase by (50±25)%, while emissions of other hydrocarbons are unchanged to within the estimated experimental error.

The effect of fuel preparation on time-resolved, engine-out hydrocarbon (HC) emissions over a Federal Test Procedure cycle [FTP (75CVS)] for a ULEV vehicle equipped with a 6 cylinder engine has been investigated. Using a single-cone injector, the HC mole fraction in Bag 1 increased by a factor of 3-4 during each of the three accelerations in the first 100 sec after start. No such increases were observed in Bag 3 when the engine was fully warm. The increases during accelerations in Bag 1 were reduced by a factor of 3 when using a Dual-cone fuel injector as a drop-in substitute. The total, tailpipe FTP (75CVS) mass emissions were 25% smaller when using the Dual-cone injector. These results demonstrate that fuel preparation can affect HC emissions from a vehicle very significantly during cold start as has been deduced previously during cold-start tests using a dynamometer-controlled engine.

The effect of engine operating parameters (speed, spark timing, and fuel-air equivalence ratio [Φ]) on hydrocarbon (HC) oxidation within the cylinder and exhaust system is examined using propane or isooctane fuel. Quench gas (CO2) is introduced at two locations in the exhaust system (exhaust valve or port exit) to stop the oxidation process. Increasing the speed from 1500 to 2500 RPM at MBT spark timing decreases the total, cylinder-exit HC emissions by ∼50% while oxidation in the exhaust system remains at 40% for both fuels. For propane fuel at 1500 rpm, increasing Φ from 0.9 (fuel lean) to 1.1 (fuel rich) reduces oxidation in the exhaust system from 42% to 26%; at 2500 RPM, exhaust system oxidation decreases from 40% to approximately 0% for Φ = 0.9 and 1.1, respectively. Retarded spark increases oxidation in the cylinder and exhaust system for both fuels. Decreases in total HC emissions are accompanied by increased olefinic content and atmospheric reactivity.

Modern four-valve engines are running at ever higher compression ratios in order to improve fuel efficiency. Hotter cylinder bores also can produce increased fuel economy by decreasing friction due to less viscous oil layers. In this study changes in compression ratio and coolant temperature were investigated to quantify their effect on exhaust emissions. Tests were run on a single cylinder research engine with a port-deactivated 4-valve combustion chamber. Two compression ratios (9.15:1 and 10.0:1) were studied at three air/fuel ratios (12.5, 14.6 and 16.5) at a part load condition (1500 rpm, 3.8 bar IMEP). The effect of coolant temperature (66 °C and 108°C) was studied at the higher compression ratio. The exhaust was sampled and analyzed for both total and speciated hydrocarbons. The speciation analysis provided concentration data for hydrocarbons present in the exhaust containing twelve or fewer carbon atoms.

Absorption of fuel in engine oil layers has been shown to be a possible source of hydrocarbon (HC) emissions from spark-ignited engines. However, the magnitude of this source in a normally operating engine has not been determined unambiguously. In these experiments, a series of n-alkanes of widely different solubility (n-hexane through undecane) was added (1.5 wt % each) to a Base gasoline (CA Phase 2). Steady-state experiments were carried out at two coolant temperatures (339 and 380 K) using a single-cylinder engine with the combustion chamber of a production V-8. Both total and speciated engine-out HC emissions were measured. The emissions indices of the heavier dopants did not increase relative to hexane at either coolant temperature.

This paper explores the extent to which standard dilution tunnel measurements of motor vehicle exhaust particulate matter modify particle number and size. Steady state size distributions made directly at the tailpipe, using an ejector pump, are compared to dilution tunnel measurements for three configurations of transfer hose used to transport exhaust from the vehicle tailpipe to the dilution tunnel. For gasoline vehicles run at a steady 50 - 70 mph, ejector pump and dilution tunnel measurements give consistent results of particle size and number when using an uninsulated stainless steel transfer hose. Both methods show particles in the 10 - 100 nm range at tailpipe concentrations of the order of 104 particles/cm3.

As motor vehicle emissions have been reduced to meet requirements of the clean air acts, they have become low enough to be difficult to measure accurately. This is especially the case for hydrocarbons, because after warm-up, there are fewer hydrocarbons emitted from a modern vehicle's tailpipe than in the surrounding air. It is therefore important to correctly compensate for the ambient hydrocarbon levels of the air used to dilute the collected exhaust. In estimating the accuracy of the federally required testing procedures, previously published error analyses have examined the effects of random errors. This study examines the systematic errors inherent in the CVS (Constant Volume Sampling) technique specified in federal regulations, estimates their sizes, and proposes a method using proportional ambient sampling whereby they can be avoided.

The requirement of reducing HC emissions during cold start and improving transient performance has prompted a study of the fuel injection process. Port-fuel-injection with the Intake-valve open using small droplets is a potentially feasible option to achieve the goals. To gain a better understanding of the injection process, the effects of droplet size, injection timing, and coolant temperature on the total and speciated HC emissions were tested In a Single-cylinder engine. It was found that droplet size plays an important role in the total HC emission increase during open-valve injection, especially with cold operation. Large droplets (300 μm SMD) produced a substantial HC increase while small droplets (14 μm SMD) produced no observable increase. Increase In the total HC emissions was always accompanied by an increase in the heavy fuel components in the exhaust gases.